The ‘Consent to Research’ paradigm in critical care: challenges and potential solutions

[1]  J. Marshall,et al.  Quantifying Threats to the Feasibility of Clinical Trials in Critically Ill Patients. , 2009, ATS 2009.

[2]  D. Cook,et al.  Investigator-led clinical research consortia: The Canadian Critical Care Trials Group , 2009, Critical care medicine.

[3]  Denis Xavier,et al.  Randomized Trials in Vulnerable Populations , 2008, Clinical trials.

[4]  M. Mitka.  Aiding emergency research aim of report on exceptions to informed consent. , 2007, JAMA.

[5]  F. Lemaire.  Emergency research: only possible if consent is waived? , 2007, Current opinion in critical care.

[6]  É. Azoulay,et al.  Ability of family members to predict patient's consent to critical care research , 2007, Intensive Care Medicine.

[7]  D. Elbourne,et al.  Informed consent in clinical trials in critical care: experience from the PAC-Man Study , 2006, Intensive Care Medicine.

[8]  D. Wendler,et al.  The accuracy of surrogate decision makers: a systematic review. , 2006, Archives of internal medicine.

[9]  Sylvie Chevret,et al.  Risk of post-traumatic stress symptoms in family members of intensive care unit patients. , 2005, American journal of respiratory and critical care medicine.

[10]  D. Annane,et al.  The effect of waiving consent on enrollment in a sepsis trial , 2004, Intensive Care Medicine.

[11]  L. Ackerson,et al.  Do surrogate decision makers provide accurate consent for intensive care research? , 2001, Chest.

[12]  S Chevret,et al.  Half the families of intensive care unit patients experience inadequate communication with physicians , 2000, Critical care medicine.